Synthetic methylmalonyl-CoA mutase transgene for the treatment of MUT class methylmalonic acidemia (MMA)

ABSTRACT

Synthetic polynucleotides encoding human methylmalonyl-CoA mutase (synMUT) and exhibiting augmented expression in cell culture and/or in a subject are described herein. An adeno-associated viral (AAV) gene therapy vector encoding synMUT under the control of a liver-specific promoter (AAV2/8-HCR-hAAT-synMUT-RBG) successfully rescued the neonatal lethal phenotype displayed by methylmalonyl-CoA mutase-deficient mice, lowered circulating methylmalonic acid levels in the treated animals, and resulted in prolonged hepatic expression of the product of synMUT transgene in vivo, human methylmalonyl-CoA mutase (MUT).

PRIORITY DATA

This application is a continuation of U.S. patent application Ser. No. 15/633,964, filed Jun. 27, 2017, which is a continuation of U.S. patent application Ser. No. 14/773,885, filed on Sep. 9, 2015, which issued as U.S. Pat. No. 9,719,080 on Aug. 1, 2017, which is a national phase entry pursuant to 35 U.S.C. § 371 of International Patent Application No. PCT/US2014/028045, filed Mar. 14, 2014, which application claims the benefit of U.S. Provisional Application No. 61/792,081, filed Mar. 15, 2013, the entire disclosures of which are hereby incorporated by reference.

STATEMENT OF GOVERNMENT INTEREST

The instant application was made with government support; the government has certain rights in this invention.

SEQUENCE LISTING DATA

The Sequence Listing text document filed herewith, created Feb. 20, 2014, size 13 kilobytes, and named “6137NHGRI6PCT_Sequence_Listing_ST25.txt,” is incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

The subject invention relates to engineering of the human methylmalonyl-coA mutase gene so as to enhance its expression in eukaryotic cells. Compared to the natural human MUT gene, the subject synthetic gene sequences (synMUT) are codon-optimized to enhance expression upon administration.

BACKGROUND

Methylmalonic acidemia (MMA) is an autosomal recessive disorder caused by defects in the mitochondrial localized enzyme methylmalonyl-CoA mutase (MUT) (Manoli, et al. 2010 Methylmalonic Acidemia (in Gene Reviews, eds. Pagon, et al.)). The estimated incidence of MMA is 1 in 25,000-48,000. MUT is an enzyme that catalyzes the conversion of L-methylmalonyl-CoA to succinyl-CoA. This reaction is one of several enzymatic reactions required to metabolize branch chain amino acids, odd chain fatty acids, and propionate produced by the gut flora (Chandler, et al. 2005 Mol Genet Metab 86:34-43). MUT deficiency, the most common cause of MMA, is characterized by the accumulation of methylmalonic acid and other disease-related metabolites. The disease is managed with dietary restriction of amino acid precursors and cofactors but lacks definitive therapy. MMA can lead to metabolic instability, seizures, strokes, and kidney failure, and it can be lethal even when patients are being properly managed, underscoring the need for new therapies for this disease. Even though MMA is rare, all babies born in the USA are screened for this condition as newborns, emphasizing the need to develop better therapies.

SUMMARY

As discussed above, the only treatments for MMA currently available are dietary restrictions. Patients still become metabolically unstable while on diet restriction and experience disease progression, despite medical therapy. These episodes result in numerous hospitalizations and can be fatal. The synthetic human methylmalonyl-CoA mutase (synMUT) transgene can be used as a drug, via viral- or non-viral mediated gene delivery, to restore MUT function in MMA patients, prevent metabolic instability, and ameliorate disease progression. Because this enzyme may also be important in other disorders of branched chain amino acid oxidation, gene delivery of synthetic MUT gene could be used to treat conditions other than MUT MMA.

Additionally, the synMUT transgene can be used for the in vitro production of MUT for use in enzyme replacement therapy for MMA. Enzyme replacement therapy is accomplished by administration of the synthetic MUT protein orally, sub-cutaneously, intra-muscularly, intravenously, or by other therapeutic delivery routes.

Thus, in one aspect, the invention is directed to a synthetic methylmalonyl-CoA mutase (MUT) polynucleotide (synMUT) selected from the group consisting of:

-   -   a) a polynucleotide comprising the nucleic acid sequence of SEQ.         ID NO:1;     -   b) a polynucleotide having the nucleic acid sequence of SEQ ID         NO:1;     -   c) a polynucleotide having a nucleic acid sequence with at least         about 80% identity to the nucleic acid sequence of SEQ ID NO:1;     -   d) a polynucleotide encoding a polypeptide having the amino acid         sequence of SEQ ID NO:3 or an amino acid sequence substantially         identical to the amino acid sequence of SEQ ID NO:3, wherein the         polynucleotide does not have the nucleic acid sequence of SEQ ID         NO:3; and     -   e) a polynucleotide encoding an active fragment of the         methylmalonyl-CoA mutase (MUT) protein, wherein the         polynucleotide in its entirety does not share 100% identity with         a portion of the nucleic acid sequence of SEQ ID NO:3.

In one embodiment, the fragment includes only amino acid residues 33-750, which is encoded between nucleotides 63-2250 in synMUT, and which represents the active, processed form of MUT.

By active can be meant, for example, the enzyme's ability to catalyze the isomerization of methylmalonyl-CoA to succinyl-CoA. The activity can be assayed using methods well-known in the art (as described in the context of protein function, below).

In one embodiment of a synthetic polynucleotide according to the invention, the nucleic acid sequence encodes a polypeptide having the amino acid sequence of SEQ ID NO:2 or an amino acid sequence with at least about 90% identity to the amino acid sequence of SEQ ID NO:2.

In another embodiment, the synthetic polynucleotide exhibits augmented expression relative to the expression of naturally occurring human methylmalonyl-CoA mutase polynucleotide sequence (SEQ ID NO:3) in a subject. In yet another embodiment, the synthetic polynucleotide having augmented expression comprises a nucleic acid sequence comprising codons that have been optimized relative to the naturally occurring human methylmalonyl-CoA mutase polynucleotide sequence (SEQ ID NO:3). In still another embodiment of a synthetic polynucleotide according to the invention, the nucleic acid sequence has at least about 80% of less commonly used codons replaced with more commonly used codons.

In one embodiment of a synthetic polynucleotide according to the invention, the polynucleotide is a polynucleotide having a nucleic acid sequence with at least about 85% identity to the nucleic acid sequence of SEQ ID NO:1. In another embodiment, the polynucleotide is a polynucleotide having a nucleic acid sequence with at least about 90% identity to the nucleic acid sequence of SEQ ID NO:1. In still another embodiment, the polynucleotide is a polynucleotide having a nucleic acid sequence with at least about 95% identity to the nucleic acid sequence of SEQ ID NO:1.

In one embodiment of a synthetic polynucleotide according to the invention, the nucleic acid sequence is a DNA sequence. In another embodiment, the nucleic acid sequence is a RNA sequence or peptide modified nucleic acid sequence. In another embodiment, the synthetic polynucleotide according to the invention encodes an active MUT fragment, amino acids 33-750 of synMUT, corresponding to base pairs 67-2250 in synMUT.

In another aspect, the invention is directed to an expression vector comprising the herein-described synthetic polynucleotide. In another embodiment of a vector according to the invention, the synthetic polynucleotide is operably linked to an expression control sequence. In still another embodiment, the synthetic polynucleotide is codon-optimized.

In a further aspect, the invention is directed to a method of treating a disease or condition mediated by methylmalonyl-CoA mutase or low levels of methylmalonyl-CoA mutase activity, the method comprising administering to a subject the herein-described synthetic polynucleotide.

In still a further aspect, the invention is directed to a method of treating a disease or condition mediated by methylmalonyl-CoA mutase, the method comprising administering to a subject a methylmalonyl-CoA mutase produced using the synthetic polynucleotide described herein. In another embodiment of a method of treatment according to the invention, the disease or condition is methylmalonic acidemia (MMA).

In one aspect, the invention is directed to a composition comprising the synthetic polynucleotide of claim 1 and a pharmaceutically acceptable carrier.

In another aspect, the invention is directed to a transgenic animal whose genome comprises a polynucleotide sequence encoding methylmalonyl-CoA mutase or a functional fragment thereof. In still another aspect, the invention is directed to a method for producing such a transgenic animal, comprising: providing an exogenous expression vector comprising a polynucleotide comprising a promoter operably linked to a polynucleotide encoding methylmalonyl-CoA mutase or a functional fragment thereof; introducing the vector into a fertilized oocyte; and transplanting the oocyte into a female animal.

In one aspect, the invention is directed to a transgenic animal whose genome comprises the synthetic polynucleotide described herein. In another aspect, the invention is directed to a method for producing such a transgenic animal, comprising: providing an exogenous expression vector comprising a polynucleotide comprising a promoter operably linked to the synthetic polynucleotide described herein; introducing the vector into a fertilized oocyte; and transplanting the oocyte into a female animal.

Methods for producing transgenic animals are known in the art and include, without limitation, transforming embryonic stem cells in tissue culture, injecting the transgene into the pronucleus of a fertilized animal egg (DNA microinjection), genetic/genome engineering, viral delivery (for example, retrovirus-mediated gene transfer).

Transgenic animals according to the invention include, without limitation, rodent (mouse, rat, squirrel, guinea pig, hamster, beaver, porcupine), frog, ferret, rabbit, chicken, pig, sheep, goat, cow primate, and the like.

In another aspect, the invention is directed to the preclinical amelioration or rescue from the disease state, for example, methylmalonic acidemia, that the afflicted subject exhibits. This may include symptoms, such as lethargy, lethality, metabolic acidosis, and biochemical perturbations, such as increased levels of methylmalonic acid in blood, urine, and body fluids.

In still another aspect, the invention is directed to a method for producing a genetically engineered animal as a source of recombinant synMUT. In another aspect, genome editing, or genome editing with engineered nucleases (GEEN) may be performed with the synMUT nucleotides of the present invention allowing synMUT DNA to be inserted, replaced, or removed from a genome using artificially engineered nucleases. Any known engineered nuclease may be used such as Zinc finger nucleases (ZFNs), Transcription Activator-Like Effector Nucleases (TALENs), the CRISPR/Cas system, and engineered meganuclease re-engineered homing endonucleases. Alternately, the nucleotides of the present invention including synMUT, in combination with a CASP/CRISPR, ZFN, or TALEN can be used to engineer correction at the locus in a patient's cell either in vivo or ex vivo, then, in one embodiment, use that corrected cell, such as a fibroblast or lymphoblast, to create an iPS or other stem cell for use in cellular therapy.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates the list of codon frequencies in the human proteome.

FIG. 2 illustrates a codon-optimized synMUT (SEQ ID NO:1) of the subject invention.

FIG. 3 illustrates naturally occurring Homo sapiens MUT amino acid sequence (SEQ ID NO:2) and naturally occurring Homo sapiens MUT gene (SEQ ID NO:3).

FIG. 4 illustrates an alignment of MUT (SEQ ID NO:3) with the subject codon-optimized synMUT sequence (SEQ ID NO:1).

FIG. 5 illustrates the exonic variants seen in MUT that are present in synMUT. The numeral 1 displayed indicate changes seen in MUT in an exome analysis that are found in synMUT. The numeral 2 displayed in the figure indicates unique synMUT variants at a position where MUT variants exist.

FIG. 6 illustrates the expression of MUT protein following transfection of HEK-293 cells in vitro with green fluorescent protein (GFP), optimized human methylmalonyl-CoA mutase polynucleotide (synMUT) (SEQ ID NO:1), or naturally-occurring human methylmalonyl-CoA mutase gene (MUT) (SEQ ID NO:3).

FIG. 7 presents a map of the AAV-HCR-hAAT-synMUT construct.

FIG. 8 illustrates the increased survival of Mut^(−/−) mice after treatment with the AAV8-HCR-hAAT-synMUT construct.

FIG. 9 illustrates the reduction in circulating metabolites in Mut^(−/−) mice after treatment with the AAV8-HCR-hAAT-synMUT construct.

FIG. 10 shows expression of MUT in the liver after AAV8-HCR-hAAT-synMUT gene therapy.

FIG. 11 shows an incidence of hepatocellular carcinoma following AAV Delivery-Mut+/− mice were either untreated (n=51), treated with 1-2×10¹¹ GC of AAV8-CBA-MUT (n=13) or 1-2×10¹¹ GC of AAV8-hAAT-synMUT (n=5) by intrahepatic injection at birth. *=P<0.01, NS=not statistically significant from untreated control group.

DETAILED DESCRIPTION

Reference will now be made in detail to representative embodiments of the invention. While the invention will be described in conjunction with the enumerated embodiments, it will be understood that the invention is not intended to be limited to those embodiments. On the contrary, the invention is intended to cover all alternatives, modifications, and equivalents that may be included within the scope of the present invention as defined by the claims.

One skilled in the art will recognize many methods and materials similar or equivalent to those described herein, which could be used in and are within the scope of the practice of the present invention. The present invention is in no way limited to the methods and materials described.

All publications, published patent documents, and patent applications cited in this application are indicative of the level of skill in the art(s) to which the application pertains. All publications, published patent documents, and patent applications cited herein are hereby incorporated by reference to the same extent as though each individual publication, published patent document, or patent application was specifically and individually indicated as being incorporated by reference.

Definitions

Unless defined otherwise, technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods, devices, and materials similar or equivalent to those described herein can be used in the practice or testing of the invention, the preferred methods, devices, and materials are now described.

As used in this application, including the appended claims, the singular forms “a,” “an,” and “the” include plural references, unless the content clearly dictates otherwise, and are used interchangeably with “at least one” and “one or more.” Thus, reference to “a polynucleotide” includes a plurality of polynucleotides or genes, and the like.

As used herein, the term “about” represents an insignificant modification or variation of the numerical value such that the basic function of the item to which the numerical value relates is unchanged.

As used herein, the terms “comprises,” “comprising,” “includes,” “including,” “contains,” “containing,” and any variations thereof, are intended to cover a non-exclusive inclusion, such that a process, method, product-by-process, or composition of matter that comprises, includes, or contains an element or list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, product-by-process, or composition of matter.

In the context of synMUT, the terms “gene” and “transgene” are used interchangeably. A “transgene” is a gene that has been transferred from one organism to another.

The term “subject”, as used herein, refers to a domesticated animal, a farm animal, a primate, a mammal, for example, a human.

The phrase “substantially identical”, as used herein, refers to an amino acid sequence exhibiting high identity with a reference amino acid sequence (for example, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, or at least 99% identity) and retaining the biological activity of interest (the enzyme activity).

The polynucleotide sequences encoding synMUT allow for increased expression of the synMUT gene relative to naturally occurring human MUT sequences. These polynucleotide sequences are designed to not alter the naturally occurring human MUT amino acid sequence. They are also engineered or optimized to have increased transcriptional, translational, and protein refolding efficacy. This engineering is accomplished by using human codon biases, evaluating GC, CpG, and negative GpC content, optimizing the interaction between the codon and anti-codon, and eliminating cryptic splicing sites and RNA instability motifs. Because the sequences are novel, they facilitate detection using nucleic acid-based assays.

As used herein, “MUT” refers to human methylmalonyl coenzyme A mutase, and “Mut” refers to mouse methylmalonyl coenzyme A mutase. This protein catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA. This process requires 5′-deoxyadenosylcobalamin, a vitamin B12 derivative. Succinyl-CoA is a component of the citric acid cycle or tricarboxylic acid cycle (TCA). The gene encoding naturally occurring human methylmalonyl coenzyme A mutase gene is referred to as MUT. The polynucleotide encoding synthetic MUT is known as synMUT.

Naturally occurring human MUT is referred to as MUT, while synthetic MUT is designated as synMUT, even though the two are identical at the amino acid level.

“Codon optimization” refers to the process of altering a naturally occurring polynucleotide sequence to enhance expression in the target organism, e.g., humans. In the subject application, the human MUT gene has been altered to replace codons that occur less frequently in human genes with those that occur more frequently and/or with codons that are frequently found in highly expressed human genes.

As used herein, “determining”, “determination”, “detecting”, or the like are used interchangeably herein and refer to the detecting or quantitation (measurement) of a molecule using any suitable method, including immunohistochemistry, fluorescence, chemiluminescence, radioactive labeling, surface plasmon resonance, surface acoustic waves, mass spectrometry, infrared spectroscopy, Raman spectroscopy, atomic force microscopy, scanning tunneling microscopy, electrochemical detection methods, nuclear magnetic resonance, quantum dots, and the like. “Detecting” and its variations refer to the identification or observation of the presence of a molecule in a biological sample, and/or to the measurement of the molecule's value.

As used herein, a “pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible. Examples of pharmaceutically acceptable carriers include one or more of water, saline, phosphate buffered saline, dextrose, glycerol, ethanol and the like, as well as combinations thereof. In certain embodiments, it may be preferable to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, or sodium chloride in the composition.

A “therapeutically effective amount” refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired therapeutic result. A therapeutically effective amount of a vector comprising the synthetic polynucleotide of the invention may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the vector to elicit a desired response in the individual. A therapeutically effective amount is also one in which any toxic or detrimental effects of the vector are outweighed by the therapeutically beneficial effects. A “prophylactically effective amount” refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired prophylactic result. Typically, since a prophylactic dose is used in subjects prior to or at an earlier stage of disease, the prophylactically effective amount will be less than the therapeutically effective amount.

Dosage regimens may be adjusted to provide the optimum desired response (e.g., a therapeutic or prophylactic response). For example, a single bolus may be administered, several divided doses may be administered over time, or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the mammalian subjects to be treated; each unit containing a predetermined quantity of the synthetic polynucleotide or a fragment thereof according to the invention calculated to produce the desired therapeutic effect in association with a pharmaceutical carrier.

Additional Embodiments of the Invention

The Synthetic Polynucleotide

In one embodiment of the invention, codon optimization was employed to create a highly active and synthetic MUT allele. This method involves determining the relative frequency of a codon in the protein-encoding genes in the human genome. For example, isoleucine can be encoded by AUU, AUC, or AUA, but in the human genome, AUC (47%), AUU (36%), and AUA (17%) are variably used to encode isoleucine in proteins. Therefore, in the proper sequence context, AUA would be changed to AUC to allow this codon to be more efficiently translated in human cells. FIG. 1 presents the codon usage statistics for a large fraction of human protein-encoding genes and serves as the basis for changing the codons throughout the MUT cDNA.

Thus, the invention comprises synthetic polynucleotides encoding methylmalonyl-CoA mutase (MUT) selected from the group consisting of the nucleic acid sequence of FIG. 2 (SEQ ID NO:1) and a polynucleotide sequence having at least about 80% identity thereto. For those polynucleotides having at least about 80% identity to SEQ ID NO:1, in additional embodiments, they have at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, or at least 99% identity.

In one embodiment, the subject synthetic polynucleotide encodes a polypeptide with 100% identity to the naturally occurring human MUT protein, alternatively including naturally occurring alleles (FIG. 3). BLASTN alignment of MUT (NM_000255.3) with synMUT reveals 1721/2253 (76%) identities (FIG. 4); 532 bases are present in synMUT and not in MUT (NM_000255.3) (FIG. 4). To further validate that the synMUT sequence selected was sufficiently unique, 8600 exomes deposited in the NHLBI exome variant server (http://evs.gs.washington.edu/EVS/) were analyzed using NCBI's Align Specialized BLAST to compare the two sequences. 67 naturally occurring nucleotide changes in the MUT coding sequence resulted in synonymous alleles, missense variants, and missense mutations (Table 1). At nine of these 67 variant locations, synMUT possessed unique nucleotides that were not present in the exome database (FIG. 5). The synMUT therefore encodes 58 variants, present at variable frequencies (Table 1), identified in the exome database, and 474 unique base pairs, not present in the 8600 human exomes compared to MUT (NM_000255.3).

TABLE 1 Variants in syn-MUT not observed in the Exome data base Allele Present Allelles on Non- Coding Coding Strand Variant Strand syn- All GVS Amino Protein cDNA Position Bases MUT Allele # MAF (%) Function Acid Pos. Pos. 6: 49427127 C/T A C = 1/T = 13005 0.0116/0.0/0.0077 missense ARG, GLN  18/751 53 6: 49427030 G/C G G = 1/C = 13005 0.0/0.0227/0.0077 missense HIS, GLN  50/751 150 6: 49426975 C/T A C = 39/T = 12967 0.3837/0.1362/0.2999 missense VAL, ILE  69/751 205 6: 49426939 G/A C G = 1/A = 13005 0.0116/0.0/0.0077 coding- none  81/751 241 synonymous 6: 49426895 C/T T C = 3/T = 13003 0.0/0.0681/0.0231 coding- none  95/751 285 synonymous 6: 49426896 A/G A = 3/G = 13003 0.0/0.0681/0.0231 missense LEU, PRO  95/751 284 6: 49426853 T/C G T = 1/C = 13005 0.0116/0.0/0.0077 coding- none 109/751 327 synonymous 6: 49426814 C/G T C = 1/G = 13005 0.0116/0.0/0.0077 missense LEU, PHE 122/751 366 6: 49425764 T/C G T = 15/C = 12989 0.0/0.3404/0.1153 coding- none 131/751 393 synonymous 6: 49425601 C/T A C = 1/T = 13005 0.0116/0.0/0.0077 missense VAL, MET 186/751 556 6: 49425591 C/T A C = 3/T = 13003 0.0/0.0681/0.0231 missense SER, ASN 189/751 566 6: 49425537 A/C G A = 1/C = 13005 0.0/0.0227/0.0077 missense VAL, GLY 207/751 620 6: 49425521 T/C A T = 7823/C = 5181 38.3578/42.7372/39.8416 coding- none 212/751 636 synonymous 6: 49425446 C/T A C = 138/T = 12854 1.3388/0.5225/1.0622 coding- none 237/751 711 synonymous 6: 49425436 C/T A C = 1/T = 12995 0.0/0.0227/0.0077 missense VAL, ILE 241/751 721 6: 49423948 A/G C A = 1/G = 13003 0.0116/0.0/0.0077 coding- none 252/751 756 synonymous 6: 49423923 C/T A C = 1/T = 13005 0.0/0.0227/0.0077 missense VAL, ILE 261/751 781 6: 49423868 C/T A C = 12/T = 12994 0.0/0.2724/0.0923 missense CYS, TYR 279/751 836 6: 49423826 C/T A C = 13/T = 12993 0.1395/0.0227/0.1 missense ARG, GLN 293/751 878 6: 49421373 T/C G T = 2/C = 13004 0.0/0.0454/0.0154 missense ILE, MET 336/751 1008 6: 49421345 T/G C T = 1/G = 13005 0.0/0.0227/0.0077 missense ILE, LEU 346/751 1036 6: 49419403 G/T A G = 1/T = 13005 0.0/0.0227/0.0077 missense PRO, THR 370/751 1108 6: 49419396 G/A T G = 6/A = 13000 0.0698/0.0/0.0461 missense THR, ILE 372/751 1115 6: 49419386 T/C G T = 22/C = 12984 0.2442/0.0227/0.1692 missense ILE, MET 375/751 1125 6: 49419305 C/A T C = 1/A = 13005 0.0/0.0227/0.0077 coding- none 402/751 1206 synonymous 6: 49419241 A/G C A = 1/G = 13005 0.0/0.0227/0.0077 missense SER, PRO 424/751 1272 6: 49419214 G/A T G = 1/A = 13005 0.0116/0.0/0.0077 missense ARG, CYS 433/751 1297 6: 49419206 A/T A A = 1/T = 13005 0.0116/0.0/0.0077 coding- none 435/751 1305 synonymous 6: 49416573 T/C G T = 1/C = 13005 0.0116/0.0/0.0077 missense GLN, ARG 467/751 1400 6: 49416571 C/T A C = 1/T = 13005 0.0116/0.0/0.0077 missense VAL, ILE 468/751 1402 6: 49416556 A/C G A = 2/C = 13004 0.0233/0.0/0.0154 missense SER, ALA 473/751 1417 6: 49416552 T/C G T = 1/C = 13005 0.0/0.0227/0.0077 missense GLN, ARG 474/751 1421 6: 49415450 C/T A C = 1/T = 12997 0.0116/0.0/0.0077 missense GLY, ASP 498/751 1493 6: 49415448 T/C G T = 1343/C = 11655 10.5655/9.8774/10.3324 missense THR, ALA 499/751 1495 6: 49415432 C/G C C = 1/G = 12999 0.0/0.0227/0.0077 missense GLY, ALA 504/751 1511 6: 49415384 G/T A G = 1/T = 12997 0.0116/0.0/0.0077 missense-near- THR, LYS 520/751 1559 splice 6: 49412463 C/T A C = 1/T = 13005 0.0116/0.0/0.0077 missense ARG, LYS 522/751 1566 6: 49412458 C/T T C = 1/T = 13005 0.0/0.0227/0.0077 missense GLY, SER 524/751 1570 6: 49412433 T/C G T = 4077/C = 8929 36.6047/21.0849/31.3471 missense HIS, ARG 532/751 1595 6: 49412430 T/C G T = 1/C = 13005 0.0116/0.0/0.0077 missense TYR, CYS 533/751 1598 6: 49412421 A/G C A = 1/G = 13005 0.0/0.0227/0.0077 missense VAL, ALA 536/751 1607 6: 49412399 A/G C A = 56/G = 12950 0.6047/0.0908/0.4306 coding- none 543/751 1629 synonymous 6: 49412398 T/C G T = 1/C = 13005 0.0/0.0227/0.0077 missense ARG, GLY 544/751 1630 6: 49409627 T/C C T = 1/C = 13005 0.0/0.0227/0.0077 coding- none 578/751 1734 synonymous 6: 49409598 A/C G A = 3/C = 13003 0.0/0.0681/0.0231 missense LEU, ARG 588/751 1763 6: 49409599 A/G A A = 16/G = 12990 0.0/0.3631/0.123 missense CYS, ARG 588/751 1762 6: 49409584 G/C G G = 2/C = 13004 0.0/0.0454/0.0154 missense GLN, GLU 593/751 1777 6: 49409569 C/T A C = 2/T = 13004 0.0/0.0454/0.0154 missense ALA, THR 598/751 1792 6: 49408037 T/C A T = 1/C = 13005 0.0/0.0227/0.0077 missense HIS, ARG 613/751 1839 6: 49408008 T/C G T = 1/C = 13005 0.0/0.0227/0.0077 missense ARG, GLY 623/751 1867 6: 49407995 C/T A C = 1/T = 13005 0.0116/0.0/0.0077 missense ARG, HIS 627/751 1880 6: 49407986 T/C G T = 1/C = 13005 0.0116/0.0/0.0077 missense GLU, GLY 630/751 1889 6: 49403334 G/A A G = 1/A = 13005 0.0116/0.0/0.0077 coding- none 653/751 1959 synonymous 6: 49403324 A/C G A = 1/C = 13005 0.0/0.0227/0.0077 missense LEU, VAL 657/751 1969 6: 49403301 T/C T T = 21/C = 12985 0.0465/0.3858/0.1615 coding- none 664/751 1992 synonymous 6: 49403302 A/G C A = 6/G = 13000 0.0698/0.0/0.0461 missense VAL, ALA 664/751 1991 6: 49403282 C/T G C = 7894/T = 5112 38.3256/41.2165/39.3049 missense VAL, ILE 671/751 2011 6: 49403268 G/A A G = 1/A = 13005 0.0116/0.0/0.0077 coding- none 675/751 2025 synonymous 6: 49403270 T/C G T = 1/C = 13005 0.0/0.0227/0.0077 missense THR, ALA 675/751 2023 6: 49403267 T/C G T = 1/C = 13005 0.0/0.0227/0.0077 missense THR, ALA 676/751 2026 6: 49403260 C/T A C = 1/T = 13005 0.0/0.0227/0.0077 missense ARG, HIS 678/751 2033 6: 49403194 T/A T T = 1/A = 13005 0.0116/0.0/0.0077 missense LYS, MET 700/751 2099 6: 49399544 A/C G A = 3/C = 13003 0.0/0.0681/0.0231 missense VAL, GLY 717/751 2150 6: 49399498 A/G A A = 1/G = 13005 0.0116/0.0/0.0077 coding- none 732/751 2196 synonymous 6: 49399476 T/C G T = 1/C = 13005 0.0116/0.0/0.0077 missense LYS, GLU 740/751 2218

In another aspect, SEQ ID NO:3 encodes MUT protein that has 100% identity with the naturally occurring human MUT protein, or that has at least 90% amino acid identity to the naturally occurring human MUT protein. In a preferred embodiment, the polynucleotide encodes MUT protein that has at least 95% amino acid identity to naturally occurring human MUT protein.

In one embodiment, a polypeptide according to the invention retains at least 90% of the naturally occurring human MUT protein function, i.e., the capacity to catalyze the conversion of L-methylmalonyl-CoA to succinyl-CoA. In another embodiment, the encoded MUT protein retains at least 95% of the naturally occurring human MUT protein function. This protein function can be measured, for example, via the efficacy to rescue a neonatal lethal phenotype in Mut knock-out mice (Chandler, et al. 2010 Mol Ther 18:11-6) (FIG. 9), the lowering of circulating metabolites including methylmalonic acid in a disease model of MMA (Chandler, et al. 2010 Mol Ther 18:11-6; Carrillo-Carrasco, et al. 2010 Hu Gene Ther 21:1147-54; Senac, et al. 2012 Gene Ther 19:385-91) (FIG. 10), the measurement of whole body (Chandler, et al. 2010 Mol Ther 18:11-6; Senac, et al. 2012 Gene Ther 19:385-91) or hepatic ¹—C—¹³ propionate oxidative capacity (Carrillo-Carrasco, et al. 2010 Hu Gene Ther 21:1147-54), or the correction of macromolecular ¹—C—¹⁴ propionate incorporation in cell culture (Chandler, et al. 2007 BMC Med Genet 8:64).

In some embodiments, the synthetic polynucleotide exhibits improved expression relative to the expression of naturally occurring human methylmalonyl-CoA mutase polynucleotide sequence. The improved expression is due to the polynucleotide comprising codons that have been optimized relative to the naturally occurring human methylmalonyl-CoA mutase polynucleotide sequence. In one aspect, the synthetic polynucleotide has at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80% of less commonly used codons replaced with more commonly used codons. In additional embodiments, the polynucleotide has at least 85%, 90%, or 95% replacement of less commonly used codons with more commonly used codons, and demonstrate equivalent or enhanced expression of MUT as compared to SEQ ID NO:3

In some embodiments, the synthetic polynucleotide sequences of the invention preferably encode a polypeptide that retains at least about 80% of the enhanced MUT expression (as demonstrated by expression of the polynucleotide of SEQ ID NO:1 in an appropriate host.) In additional embodiments, the polypeptide retains at least 85%, 90%, or 95% or 100% of the enhanced expression observed with the polynucleotide of SEQ ID NO:1.

In designing the synMUT of the present invention, the following considerations were balanced. For example, the fewer changes that are made to the nucleotide sequence of SEQ ID NO:3, decreases the potential of altering the secondary structure of the sequence, which can have a significant impact on gene expression. The introduction of undesirable restriction sites is also reduced, facilitating the subcloning of MUT into the plasmid expression vector. However, a greater number of changes to the nucleotide sequence of SEQ ID NO:3 allows for more convenient identification of the translated and expressed message, e.g. mRNA, in vivo. Additionally, greater number of changes to the nucleotide sequence of SEQ ID NO:3 provides for increased likelihood of greater expression. These considerations were balanced when arriving at SEQ ID NO:1. The polynucleotide sequences encoding synMUT allow for increased expression of the synMUT gene relative to naturally occurring human MUT sequences. They are also engineered to have increased transcriptional, translational, and protein refolding efficacy. This engineering is accomplished by using human codon biases, evaluating GC, CpG, and negative GpC content, optimizing the interaction between the codon and anti-codon, and eliminating cryptic splicing sites and RNA instability motifs. Because the sequences are novel, they facilitate detection using nucleic acid-based assays.

MUT has a total of 750 amino acids and synMUT contains approximately 750 codons corresponding to said amino acids. Of these codons, in SEQ ID NO:1, approximately 463 codons are changed from that of the natural human MUT, however, as described, SEQ ID NO:1, despite changes from SEQ ID NO:3, codes for the amino acid sequence SEQ ID NO:2 for MUT. Codons for SEQ ID NO:1 are changed, in accordance with the equivalent amino acid positions of SEQ ID NO:2, at positions 2, 4, 5, 6, 8, 9, 10, 11, 12, 13, 14, 15, 17, 18, 19, 22, 23, 24, 25, 26, 27, 29, 30, 31, 32, 33, 36, 38, 39, 40, 41, 42, 44, 45, 47, 48, 49, 52, 59, 60, 63, 64, 65, 67, 68, 69, 70, 72, 73, 74, 75, 76, 77, 80, 81, 82, 83, 85, 90, 92, 93, 95, 96, 97, 98, 100, 103, 106, 107, 108, 110, 111, 112, 113, 117, 119, 120, 122, 128, 129, 130, 134, 135, 136, 137, 138, 141, 134, 147, 149, 150, 151, 152, 153, 154, 155, 156, 157, 160, 162, 164, 166, 170, 171, 173, 174, 177, 179, 180, 183, 184, 185, 187, 189, 190, 191, 192, 194, 195, 196, 198, 199, 200, 201, 203, 204, 206, 207, 208, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 224, 225, 227, 228, 230, 234, 235, 241, 243, 244, 245, 246, 247, 248, 249, 250, 254, 255, 256, 257, 220, 262, 263, 264, 270, 271, 272, 273, 278, 279, 280, 281, 284, 285, 286, 287, 289, 290, 292, 294, 298, 299, 300, 301, 302, 303, 304, 305, 306, 308, 312, 314, 315, 316, 318, 319, 320, 323, 325, 326, 328, 330, 332, 333, 335, 337, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 355, 357, 358, 360, 362, 363, 364, 365, 369, 370, 372, 373, 377, 378, 379, 381, 382, 384, 385, 388, 389, 392, 393, 394, 395, 396, 397, 398, 400, 401, 403, 405, 406, 407, 409, 411, 412, 413, 414, 416, 417, 418, 419, 420, 422, 424, 427, 432, 433, 434, 436, 437, 438, 432, 434, 435, 439, 450, 453, 456, 457, 458, 459, 462, 463, 464, 466, 467, 468, 469, 472, 473, 474, 475, 476, 477, 478, 479, 480, 481, 482, 483, 485, 486, 487, 488, 489, 494, 495, 499, 500, 502, 504, 505, 507, 508, 509, 511, 512, 513, 516, 517, 518, 520, 523, 524, 525, 527, 528, 529, 530, 532, 533, 534, 535, 536, 537, 538, 539, 542, 544, 545, 547, 548, 551, 553, 555, 556, 558, 560, 561, 563, 566, 567, 570, 571, 572, 573, 574, 575, 576, 577, 578, 581, 584, 585, 586, 588, 590, 591, 592, 594, 597, 598, 599, 600 604, 605, 606, 609, 610, 612, 613, 614, 615, 616, 617, 618, 619, 621, 624, 625, 626, 628, 629, 633, 635, 636, 637, 638, 640, 641, 642, 644, 646, 627, 630, 633, 634, 635, 636, 637, 638, 661, 662, 663, 664, 667, 668, 669, 670, 671, 672, 673, 674, 675, 677, 679, 681, 682, 683, 686, 689, 691, 692, 693, 694, 696, 697, 698, 701, 702, 703, 705, 707, 710, 711, 714, 715, 716, 717, 718, 719, 720, 721, 722, 723, 724, 725, 726, 727, 728, 729, 731, 732, 733, 734, 735, 736, 740, 743, 745, 746, 748, 749, 750 of SEQ ID NO:2, relative to the natural human sequence SEQ ID NO:3. In this embodiment, the amino acid sequence for natural human MUT has been retained.

It can be appreciated that partial reversion of the designed synMUT to codons that are found in MUT can be expected to result in nucleic acid sequences that, when incorporated into appropriate vectors, can also exhibit the desirable properties of SEQ ID NO:1, for example, such partial reversion variants can have equivalent expression of MUT from a vector inserted into an appropriate host, as SEQ ID NO:1. For example, the invention includes nucleic acids in which at least about 1 altered codon, at least about 2 altered codons, at least about 3, altered codons, at least about 4 altered codons, at least about 5 altered codons, at least about 6 altered codons, at least about 7 altered codons, at least about 8 altered codons, at least about 9 altered codons, at least about 10 altered codons, at least about 11 altered codons, at least about 12 altered codons, at least about 13 altered codons, at least about 14 altered codons, at least about 15 altered codons, at least about 16 altered codons, at least about 17 altered codons, at least about 18 altered codons, at least about 20 altered codons, at least about 25 altered codons, at least about 30 altered codons, at least about 35 altered codons, at least about 40 altered codons, at least about 50 altered codons, at least about 55 altered codons, at least about 60 altered codons, at least about 65 altered codons, at least about 70 altered codons, at least about 75 altered codons, at least about 80 altered codons, at least about 85 altered codons, at least about 90 altered codons, at least about 95 altered codons, at least about 100 altered codons, at least about 110 altered codons, at least about 120 altered codons, at least about 130 altered codons, at least about 130 altered codons, at least about 140 altered codons, at least about 150 altered codons, at least about 160 altered codons, at least about 170 altered codons, at least about 180 altered codons, at least about 190 altered codons, at least about 200 altered codons, at least about 220 altered codons, at least about 240 altered codons, at least about 260 altered codons, at least about 280 altered codons, at least about 300 altered codons, at least about 320 altered codons, at least about 340 altered codons, at least about 360 altered codons, at least about 380 altered codons, at least about 400 altered codons, at least about 420 altered codons, at least about 440 altered codons, at least about 460 altered codons, or at least about 480 of the altered codon positions in SEQ ID NO:1 are reverted to native codons according to SEQ ID NO:3, an alternate codon sequence for an amino acid sequence as shown in FIG. 1, or to SEQ ID NO:3 containing SNPs (alleles) as noted in Table 1, and having equivalent expression to SEQ ID NO:1. Alternately, at least about 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 100% of the altered codon positions in SEQ ID NO:1 are reverted to native sequence according to SEQ ID NO:3, an alternate codon sequence for an amino acid sequence as shown in FIG. 1, or to SEQ ID NO:3 containing SNPs as noted in Table 1, and having equivalent expression to SEQ ID NO:1.

In some embodiments, polynucleotides of the present invention do not share 100% identity with SEQ ID NO:3. In other words, in some embodiments, polynucleotides having 100% identity with SEQ ID NO:3 are excluded from the embodiments of the present invention.

The synthetic polynucleotide can be composed of DNA and/or RNA or a modified nucleic acid, such as a peptide nucleic acid, and could be conjugated for improved biological properties.

Therapy

In another aspect, the invention comprises a method of treating a disease or condition mediated by methylmalonyl-CoA mutase. The disease or condition can, in one embodiment, be methylmalonic acidemia (MMA). This method comprises administering to a subject in need thereof a synthetic methylmalonyl-CoA mutase polynucleotide construct comprising the synthetic polynucleotides (synMUT) described herein. The MUT enzyme is processed after transcription, translation, and translocation into the mitochondrial inner space. During this importation and maturation process, amino acids 1-32 are removed to produce the mature MUT peptide, comprised of residues 33-750. Thus, in another embodiment, the invention includes the portion of the synMUT enzyme located inside the mitochondrial matrix, specifically, residues 33-750 corresponding to nucleotides 62-2250 of synMUT, attached to a carrier, synthetic or heterologous mitochondrial leader sequence, charged or lipophilic small molecule to direct toward the mitochondria; conjugated or covalently modified to a peptide that targets the mitochondrial matrix; or encapsulated to deliver this fragment of synMUT to a subcellular organelle, cell type or tissue.

Enzyme replacement therapy consists of administration of the functional enzyme (methylmalonyl-CoA mutase) to a subject in a manner so that the enzyme administered will catalyze the reactions in the body that the subject's own defective or deleted enzyme cannot. In enzyme therapy, the defective enzyme can be replaced in vivo or repaired in vitro using the synthetic polynucleotide according to the invention. The functional enzyme molecule can be isolated or produced in vitro, for example. Methods for producing recombinant enzymes in vitro are known in the art. In vitro enzyme expression systems include, without limitation, cell-based systems (bacterial (for example, Escherichia coli, Corynebacterium, Pseudomonas fluorescens), yeast (for example, Saccharomyces cerevisiae, Pichia Pastoris), insect cell (for example, Baculovirus-infected insect cells, non-lytic insect cell expression), and eukaryotic systems (for example, Leishmania)) and cell-free systems (using purified RNA polymerase, ribosomes, tRNA, ribonucleotides). Viral in vitro expression systems are likewise known in the art. The enzyme isolated or produced according to the above-iterated methods exhibits, in specific embodiments, 80%, 85%, 90%, 95%, 98%, 99%, or 100% homology to the naturally occurring (for example, human) methylmalonyl-CoA mutase.

Gene therapy can involve in vivo gene therapy (direct introduction of the genetic material into the cell or body) or ex vivo gene transfer, which usually involves genetically altering cells prior to administration. In one aspect, genome editing, or genome editing with engineered nucleases (GEEN) may be performed with the synMUT nucleotides of the present invention allowing synMUT DNA to be inserted, replaced, or removed from a genome using artificially engineered nucleases. Any known engineered nuclease may be used such as Zinc finger nucleases (ZFNs), Transcription Activator-Like Effector Nucleases (TALENs), the CRISPR/Cas system, and engineered meganuclease re-engineered homing endonucleases. Alternately, the nucleotides of the present invention including synMUT, in combination with a CASP/CRISPR, ZFN, or TALEN can be used to engineer correction at the locus in a patient's cell either in vivo or ex vivo, then, in one embodiment, use that corrected cell, such as a fibroblast or lymphoblast, to create an iPS or other stem cell for use in cellular therapy.

Administration/Delivery and Dosage Forms

Routes of delivery of a synthetic methylmalonyl-Co-A mutase (MUT) polynucleotide according to the invention may include, without limitation, injection (systemic or at target site), for example, intradermal, subcutaneous, intravenous, intraperitoneal, intraocular, subretinal, renal artery, hepatic vein, intramuscular injection; physical, including ultrasound(-mediated transfection), electric field-induced molecular vibration, electroporation, transfection using laser irradiation, photochemical transfection, gene gun (particle bombardment); parenteral and oral (including inhalation aerosols and the like). Related methods include using genetically modified cells, antisense therapy, and RNA interference.

Vehicles for delivery of a synthetic methylmalonyl-CoA mutase polynucleotide (synMUT) according to the invention may include, without limitation, viral vectors (for example, AAV, adenovirus, baculovirus, retrovirus, lentivirus, foamy virus, herpes virus, Moloney murine leukemia virus, Vaccinia virus, and hepatitis virus) and non-viral vectors (for example, naked DNA, mini-circules, liposomes, ligand-polylysine-DNA complexes, nanoparticles, cationic polymers, including polycationic polymers such as dendrimers, synthetic peptide complexes, artificial chromosomes, and polydispersed polymers). Thus, dosage forms contemplated include injectables, aerosolized particles, capsules, and other oral dosage forms.

In certain embodiments, the vector used for gene therapy comprises an expression cassette. The expression cassette may, for example, consist of a promoter, the synthetic polynucleotide, and a polyadenylation signal. Viral promoters include, for example, the ubiquitous cytomegalovirus immediate early (CMV-IE) promoter, the chicken beta-actin (CBA) promoter, the simian virus 40 (SV40) promoter, the Rous sarcoma virus long terminal repeat (RSV-LTR) promoter, the Moloney murine leukemia virus (MoMLV) LTR promoter, and other retroviral LTR promoters. The promoters may vary with the type of viral vector used and are well-known in the art.

In one specific embodiment, synMUT could be placed under the transcriptional control of a ubiquitous or tissue-specific promoter, with a 5′ intron, polyadenylation signal, and mRNA stability element, such as the woodchuck post-transcriptional regulatory element. The use of a tissue-specific promoter can restrict unwanted transgene expression, as well as facilitate persistent transgene expression. The therapeutic transgene could then be delivered as coated or naked DNA into the systemic circulation, portal vein, or directly injected into a tissue or organ, such as the liver or kidney. In addition to the liver or kidney, the brain, pancreas, eye, heart, lungs, bone marrow, and muscle may constitute targets for therapy. Other tissues or organs may be additionally contemplated as targets for therapy.

In another embodiment, the same synMUT expression construct could be packaged into a viral vector, such as an adenoviral vector, retroviral vector, lentiviral vector, or adeno-associated viral vector, and delivered by various means into the systemic circulation, portal vein, or directly injected into a tissue or organ, such as the liver or kidney. In addition to the liver or kidney, the brain, pancreas, eye, heart, lungs, bone marrow, and muscle may constitute targets for therapy. Other tissues or organs may be additionally contemplated as targets for therapy.

Tissue-specific promoters include, without limitation, Apo A-I, ApoE, hAAT, transthyretin, liver-enriched activator, albumin, PEPCK, and RNAP_(II) promoters (liver), PAI-1, ICAM-2 (endothelium), MCK, SMC α-actin, myosin heavy-chain, and myosin light-chain promoters (muscle), cytokeratin 18, CFTR (epithelium), GFAP, NSE, Synapsin I, Preproenkephalin, dβH, prolactin, and myelin basic protein promoters (neuronal), and ankyrin, α-spectrin, globin, HLA-DRα, CD4, glucose 6-phosphatase, and dectin-2 promoters (erythroid).

Regulable promoters (for example, ligand-inducible or stimulus-inducible promoters) are also contemplated for expression constructs according to the invention.

In yet another embodiment, synMUT could be used in ex vivo applications via packaging into a retro- or lentiviral vector to create an integrating vector that could be used to permanently correct any cell type from a patient with MUT deficiency. The synMUT-transduced and corrected cells could then be used as a cellular therapy. Examples might include CD34+ stem cells, primary hepatocytes, or fibroblasts derived from patients with MUT deficiency. Fibroblasts could be reprogrammed to other cell types using iPS methods well known to practitioners of the art. In yet another embodiment, synMUT could be recombined using genomic engineering techniques that are well known to practitioners of the art, such as ZFNs and TALENS, into the MUT locus, a genomic safe harbor site, such as AAVS1, or into another advantageous location, such as into rDNA, the albumin locus, GAPDH, or a suitable expressed pseudogene.

A composition (pharmaceutical composition) for treating an individual by gene therapy may comprise a therapeutically effective amount of a vector comprising the synMUT transgenes or a viral particle produced by or obtained from same. The pharmaceutical composition may be for human or animal usage. Typically, a physician will determine the actual dosage which will be most suitable for an individual subject, and it will vary with the age, weight, and response of the particular individual.

The composition may, in specific embodiments, comprise a pharmaceutically acceptable carrier, diluent, excipient, or adjuvant. Such materials should be non-toxic and should not interfere with the efficacy of the transgene. Pharmaceutically acceptable excipients include, but are not limited to, liquids such as water, saline, glycerol, sugars and ethanol. Pharmaceutically acceptable salts can also be included therein, for example, mineral acid salts such as hydrochlorides, hydrobromides, phosphates, sulfates, and the like; and the salts of organic acids such as acetates, propionates, malonates, benzoates, and the like. Additionally, auxiliary substances, such as wetting or emulsifying agents, pH buffering substances, and the like, may be present in such vehicles. A thorough discussion of pharmaceutically acceptable excipients is available in Remington's Pharmaceutical Sciences [Mack Pub. Co., 18th Edition, Easton, Pa. (1990)]. The choice of pharmaceutical carrier, excipient, or diluent can be selected with regard to the intended route of administration and standard pharmaceutical practice. The pharmaceutical compositions may comprise as, or in addition to, the carrier, excipient, or diluent any suitable binder(s), lubricant(s), suspending agent(s), coating agent(s), solubilizing agent(s), and other carrier agents that may aid or increase the viral entry into the target site (such as for example a lipid delivery system). For oral administration, excipients such as starch or lactose may be used. Flavoring or coloring agents may be included, as well. For parenteral administration, a sterile aqueous solution may be used, optionally containing other substances, such as salts or monosaccharides to make the solution isotonic with blood.

A composition according to the invention may be administered alone or in combination with at least one other agent, such as a stabilizing compound, which may be administered in any sterile, biocompatible pharmaceutical carrier, including, but not limited to, saline, buffered saline, dextrose, and water. The compositions may be administered to a patient alone, or in combination with other agents, modulators, or drugs (e.g., antibiotics).

The composition may be in a variety of forms. These include, for example, liquid, semi-solid and solid dosage forms, such as liquid solutions (e.g., injectable and infusible solutions), dispersions or suspensions, tablets, pills, powders, liposomes and suppositories. Additional dosage forms contemplated include: in the form of a suppository or pessary; in the form of a lotion, solution, cream, ointment or dusting powder; by use of a skin patch; in capsules or ovules; in the form of elixirs, solutions, or suspensions; in the form of tablets or lozenges.

EXAMPLES

Cell culture studies: A synthetic codon-optimized human methylmalonyl-Co-A mutase gene (synMUT) was engineered using an iterative approach, wherein the naturally occurring MUT cDNA (NCBI Reference Sequence: NM_000255.3 was optimized codon by codon to create synMUT (FIG. 2) using OptimumGene™ codon optimization software (Genscript Inc) that incorporates critical factors involved in protein expression, such as codon adaptability, mRNA structure, and various cis-elements in transcription and translation. The resulting sequence that was selected had the maximal divergence from the MUT cDNA at the nucleotide level yet retained optimally utilized codons at each position.

To improve the expression of methylmalonyl-CoA mutase and create a vector that could express the human MUT gene in a more efficient fashion, synMUT was cloned using restriction endonuclease excision and DNA ligation into an expression vector under the control of the chicken β-actin promoter (Chandler, et al. 2010 Mol Ther 18:11-6). The construct expressing either the full-length MUT or the full-length synMUT was then transfected into 293FT cells using Lipofectamine™ (Life Technologies). Cloning and transfection methods are well understood by practitioners of the art (Sambrook, Fritsch, Maniatis. Molecular Cloning: A Laboratory Manual). After 48 hours, cellular protein was extracted from the transfected cells and evaluated for methylmalonyl-CoA mutase protein expression using Western analysis (Chandler, et al. 2010 Mol Ther 18:11-6). The results show that synMUT is transcribed and translated as or more efficiently than MUT (FIG. 6). FIG. 6 shows expression of MUT protein following transfection of HEK-293 cells in vitro with synMUT. FIG. 6(A) shows schematic of the expression constructs prepared as described in Chandler, et al. 2010 Mol Ther 18:11-6. Figure (B) shows HEK-293 cells transfected with green fluorescent protein (GFP), human codon optimized methylmalonyl-CoA mutase (labeled CBA-synMUT) or human methylmalonyl-CoA mutase (labeled CBA-MUT) expression construct. Cells transfected with CBA-synMUT exhibited a significant increase in the expression of MUT in comparison to cells transfected with GFP or CBA-MUT.

Gene therapy in methylmalonyl-CoA mutase Knock-out (Mut^(−/−)) Mice. The targeted Mut allele harbors a deletion of exon 3 in the Mut gene. This exon encodes the putative substrate-binding pocket in the Mut enzyme. The Mut allele does not produce mature RNA, protein, or enzymatic activity. Mut^(−/−) mice (mice having the Mut gene knocked out (disrupted or replaced) on a mixed (C57BL/6×[129SV/Ev×FvBN]) background exhibit a semipenetrant neonatal lethal phenotype, with most mice perishing in the early neonatal period. In the instant example, the Mut^(−/−) (methylmalonyl-CoA mutase knockout) mouse is also referred to as the mouse with MMA.

Mut^(−/−) mice display massively elevated methylmalonic acid concentrations in the plasma that progressively rises to the 2 mmol/L range, until death occurs. Mut^(+/−) animals have biochemical parameters identical to Mut^(+/+) wild-type animals and were used as controls throughout. This animal model of MMA, therefore, recapitulates the severest form of the human condition—mut^(o) methylmalonic acidemia.

The synMUT polynucleotide was then used to construct a series of novel gene therapy vectors to treat mice with MMA. One vector is designed to express synMUT in the liver of the MMA mouse and used to make a recombinant adeno-associated viral vector.

The AAV2/8-HCR-hAAT-RBG vector contains transcriptional control elements from the hepatic control region (HCR) and human alpha antitrypsin promoter (hAAT), cloning sites for the insertion of a complementary DNA, and the rabbit β-globin polyadenylation (RBG) signal (FIG. 7). Terminal repeats from AAV serotype 2 flank the expression cassette. The human codon-optimized methylmalonyl-CoA mutase (synMUT) was cloned into AAV2-HCR-hAAT-RBG and packaged into rAAV8 as previously described (Chandler, et al. 2010 Mol Ther 18:11-6), purified by cesium chloride centrifugation, and titered by qPCR to make the AAV8-HCR-hAAT-synMUT-RBG vector as previously described (Chandler, et al. 2010 Mol Ther 18:11-6; Carrillo-Carrasco, et al. 2010 Hum Gene Ther 21:1147-54). Animal studies were reviewed and approved by the National Human Genome Research Institute Animal User Committee. Hepatic injections were performed on non-anesthetized neonatal mice, typically within several hours after birth. Viral particles were diluted to a total volume of 20 microliters with phosphate-buffered saline immediately before injection and were delivered into the liver parenchyma using a 32-gauge needle and transdermal approach, as previously described.

Treatment with synMUT polynucleotide delivered using an AAV (adeno-associated virus) rescued the Mur^(−/−) mice from neonatal lethality (FIG. 8), improved their growth, and lowered the levels of plasma methylmalonic acid in the blood (FIG. 9). This establishes the pre-clinical efficacy of synMUT as a treatment for MMA in vivo, including in other animal models, as well as in humans. FIG. 8 shows increased survival of Mut^(−/−) mice following treatment with AAV8-HCR-hAAT-synMUT. Mut^(−/−) mice received a single intra-hepatic injection of 1×10¹¹ GC of AAV8-HCR-hAAT-synMUT at birth. All of the treated Mut^(−/−) mice survived until day 30 and appeared normal relative to unaffected littermates. At day 30, a single treated Mut^(−/−) mouse was sacrificed to evaluate the in vivo expression of MUT (see FIG. 9). FIG. 9 shows metabolic correction after AAV8-HCR-hAAT-synMUT gene therapy. A significant reduction in the plasma MMA levels on day of life 90 were documented in Mut^(−/−) mice that received a single intra-hepatic injection of 1×10¹¹ GC of AAV8-HCR-hAAT-synMUT at birth.

A single treated Mut^(−/−) mouse was sacrificed at 30 days after treatment with AAV2/8-HCR-hAAT-synMUT-RBG to evaluate in vivo expression of MUT (FIG. 10). FIG. 10 shows hepatic expression of MUT in a rescued Mut^(−/−) mouse following treatment with AAV8-HCR-hAAT-synMUT. The liver of the treated Mut^(−/−) mouse maintained a significant amount of MUT expression 30 days after treatment with AAV8-hAAT-synMUT, but less than that of untreated wild-type mice (Mut^(+/−)). By comparison, the liver of an untreated Mut^(−/−) mouse exhibited no detectable MUT protein.

It was observed that the liver of the treated Mut^(−/−) mouse demonstrated continued expression of MUT at 30 days after treatment with AAV2/8-HCR-hAAT-synMUT-RBG, but less than that of untreated wild-type mice (Mut^(+/+)). The untreated Mut^(−/−) mouse exhibited no detectable MUT protein expression.

Safety Study in Mice.

AAV genotoxicity, specifically hepatocarcinoma (HCC) in mice following AAV gene delivery, has been reported raising concerns about the safety of AAV gene therapy. We observed a similar increase in the occurrence of HCC following the treatment of mice with an AAV8-CBA-MUT we designed (FIG. 11). However, we do not observe any significant increase in the occurrence of HCC when mice are treated in a similar manner with AAV8-hAAT-synMUT. The data demonstrate that the AAV8-hAAT-synMUT is less genotoxic and has a better safety profile than that AAV8-CBA-MUT. These findings suggest that AAV8-hAAT-synMUT is a potentially safer AAV construct for human clinical trials. 

The invention claimed is:
 1. A method of treating a disease or condition mediated by methylmalonyl-CoA mutase, comprising administering to a subject in need thereof, in vivo or by genetic alteration of cells prior to administration, a therapeutic amount of a synthetic methylmalonyl-CoA mutase (MUT) polynucleotide (synMUT) selected from the group consisting of: a) a polynucleotide comprising the nucleic acid sequence of SEQ ID NO:1; b) a codon optimized polynucleotide comprising a polynucleotide having a nucleic acid sequence with at least about 70% identity to the nucleic acid sequence of SEQ ID NO:1 and encoding a polypeptide according to SEQ ID NO:2, and having equivalent expression in a host to either SEQ ID NO:1 expression or SEQ ID NO:3 expression, wherein the codon optimized polynucleotide having at least about 70% identity to SEQ ID NO:1 does not have the nucleic acid sequence of SEQ ID NO:3.
 2. The method of claim 1, wherein the disease or condition is methylmalonic acidemia (MMA).
 3. The method of claim 1, wherein the synthetic polynucleotide is formulated with a pharmaceutically acceptable carrier.
 4. The method of claim 1, wherein the synthetic polynucleotide of claim 1 is comprised within a viral vector selected from the group consisting of an adenoviral vector, a retroviral vector, a lentiviral vector, and an adeno-associated viral vector.
 5. The method of claim 1, wherein the synthetic polynucleotide of claim 1 is placed under the transcriptional control of a ubiquitous promoter, a tissue-specific promoter or a regulable promotor.
 6. The method of claim 1, wherein the synthetic polynucleotide of claim 1 is comprised within an expression cassette wherein the expression cassette comprises a promotor, the synthetic polynucleotide, and a polyadenylation signal.
 7. The method of claim 1, wherein the synthetic polynucleotide of claim 1 is comprised within a non-viral vector selected from the group consisting of naked DNA, mini-circules, liposomes, ligand-polylysine-DNA complexes, nanoparticles, cationic polymers, synthetic peptide complexes, artificial chromosomes and polydispersed polymers.
 8. The method of claim 1, wherein the synthetic polynucleotide of claim 1 is placed under the transcriptional control of a tissue-specific promoter selected from the group consisting of Apo A-I promoter, ApoE promoter, hAAT promoter, transthyretin promoter, liver-enriched activator, albumin promoter, PEPCK promoter, RNAP_(II) promoter, PAI-1 promoter, ICAM-2 promoter, MCK promoter, SMC α-actin promoter, myosin heavy-chain promotor, myosin light-chain promotor, cytokeratin 18 promoter, CFTR promoter, GFAP promoter, NSE promoter, Synapsin I promoter, Preproenkephalin promoter, dβH promoter, prolactin promoter, myelin basic protein promoter, ankyrin promoter, α-spectrin promoter, globin promoter, HLA-DRα promoter, CD4 promoter, glucose 6-phosphatase promoter, and dectin-2 promoter.
 9. The method of claim 1, wherein the therapeutic amount of a synthetic methylmalonyl-CoA mutase (MUT) polynucleotide (synMUT) is delivered by a route of delivery selected from the group consisting of intradermal injection, subcutaneous injection, intravenous injection, intraperitoneal injection, intraocular injection, subretinal injection, renal artery injection, hepatic vein injection, intramuscular injection, ultrasound(-mediated transfection), electric field-induced molecular vibration, electroporation, transfection using laser irradiation, photochemical transfection, gene gun particle bombardment, parenteral administration and oral administration.
 10. The method of claim 4, wherein the viral vector is AAV2/8-HCR-hAAT-RBG.
 11. The method of claim 1, wherein the synthetic polynucleotide of claim 1 is inserted into a cell of the subject via genome editing on the cell of the subject using a nuclease selected from the group of zinc finger nucleases (ZFNs), transcription activator-like effector nucleases (TALENs), clustered regularly interspaced short palindromic repeats (CRISPER/cas system) and meganuclease re-engineered homing endonuclease.
 12. The method of claim 1, wherein the synthetic polynucleotide of claim 1 has at least about 80% identity to the nucleic acid sequence of SEQ ID NO:1.
 13. The method of claim 1, wherein the synthetic polynucleotide of claim 1 has at least about 90% identity to the nucleic acid sequence of SEQ ID NO:1.
 14. The method of claim 1, wherein the synthetic polynucleotide of claim 1 has at least about 95% identity to the nucleic acid sequence of SEQ ID NO:1.
 15. A method of treating a disease or condition mediated by methylmalonyl-CoA mutase, comprising administering to a subject in need thereof a therapeutic amount of a mature methylmalonyl-CoA mutase produced using a synthetic methylmalonyl-CoA mutase (MUT) polynucleotide (synMUT) selected from the group consisting of: (a) a polynucleotide comprising the nucleic acid sequence of SEQ ID NO:1; and (b) a codon-optimized polynucleotide comprising a polynucleotide having a nucleic acid sequence with at least about 70% identity to the nucleic acid sequence of SEQ ID NO: 1 and encoding a polypeptide comprising residues 33-750 of SEQ ID NO:2, and having equivalent expression in a host to either SEQ ID NO: 1 expression or SEQ ID NO:3 expression, wherein the codon-optimized polynucleotide having at least about 70% identity to SEQ ID NO:1 does not have the nucleic acid sequence of SEQ ID NO:3.
 16. The method of claim 15, wherein the disease or condition is methylmalonic academia (MMA).
 17. The method of claim 15, wherein the mature methylmalonyl-CoA mutase polypeptide is formulated with a pharmaceutically acceptable carrier.
 18. A synthetic methylmalonyl-CoA mutase (MUT) polynucleotide (synMUT) comprising a nucleic acid sequence with at least 70% identity to the nucleic acid sequence of SEQ ID NO:1, encoding a polypeptide according to SEQ ID NO:2, and having equivalent expression in a host to either SEQ ID NO:1 expression or SEQ ID NO:3 expression, wherein the synthetic polynucleotide does not have the nucleic acid sequence of SEQ ID NO:3.
 19. The synthetic polynucleotide of claim 18, wherein the synthetic polynucleotide exhibits increased expression in an appropriate host relative to the expression SEQ ID NO:3 in an appropriate host.
 20. The synthetic polynucleotide of claim 18, wherein the synthetic polynucleotide comprises a nucleic acid sequence comprising codons that have been optimized relative to the naturally occurring human methylmalonyl-CoA mutase polynucleotide sequence (SEQ ID NO:3).
 21. The synthetic polynucleotide of claim 18, wherein the synthetic polynucleotide is comprised within a viral vector selected from the group consisting of an adenoviral vector, a baculoviral vector, a retroviral vector, a lentiviral vector, a foamy viral vector, a herpes viral vector, a Moloney murine leukemia viral vector, a Vaccinia viral vector, a hepatitis viral vector, and an adeno-associated viral vector.
 22. The synthetic polynucleotide of claim 18, wherein the synthetic polynucleotide of claim 1 is comprised within a non-viral vector selected from the group consisting of naked DNA, mini-circules, liposomes, ligand-polylysine-DNA complexes, nanoparticles, cationic polymers, synthetic peptide complexes, artificial chromosomes and polydispersed polymers.
 23. The synthetic polynucleotide of claim 18, wherein the synthetic polynucleotide is comprised within an expression cassette wherein the expression cassette comprises a promotor, the synthetic polynucleotide, and a polyadenylation signal.
 24. The synthetic polynucleotide of claim 23, wherein the expression cassette further comprises a 5′ intron.
 25. The synthetic polynucleotide of claim 23, wherein the expression cassette further comprises an mRNA stability element.
 26. The synthetic polynucleotide of claim 25, wherein the mRNA stability element is the woodchuck post-transcriptional regulatory element.
 27. The synthetic polynucleotide of claim 23, wherein the expression cassette further comprises a hepatic control region.
 28. The synthetic polynucleotide of claim 23, wherein the expression cassette further comprises an inverted terminal repeat.
 29. The synthetic polynucleotide of claim 18, wherein the synthetic polynucleotide is under the transcriptional control of a ubiquitous promoter, a tissue-specific promoter or a regulable promotor.
 30. The synthetic polynucleotide of claim 29, wherein the synthetic polynucleotide is under transcriptional control of a tissue-specific promoter selected from the group consisting of Apo A-I promoter, ApoE promoter, hAAT promoter, transthyretin promoter, liver-enriched activator, albumin promoter, PEPCK promoter, RNAP_(II) promoter, PAI-1 promoter, ICAM-2 promoter, MCK promoter, SMC α-actin promoter, myosin heavy-chain promotor, myosin light-chain promotor, cytokeratin 18 promoter, CFTR promoter, GFAP promoter, NSE promoter, Synapsin I promoter, Preproenkephalin promoter, dβH promoter, prolactin promoter, myelin basic protein promoter, ankyrin promoter, α-spectrin promoter, globin promoter, HLA-DRα promoter, CD4 promoter, glucose 6-phosphatase promoter, and dectin-2 promoter.
 31. The synthetic polynucleotide of claim 29, wherein the synthetic polynucleotide is under transcriptional control of a viral promoter selected from the group consisting of the ubiquitous cytomegalovirus immediate early (CMV-IE) promoter, the chicken beta-actin (CBA) promoter, the simian virus 40 (SV40) promoter, the Rous sarcoma virus long terminal repeat (RSV-LTR) promoter, and the Moloney murine leukemia virus (MoMLV) LTR promoter.
 32. An expression vector comprising the synthetic polynucleotide of claim
 18. 33. The expression vector of claim 32, wherein the expression vector is AAV2/8-HCR-hAAT-RBG. 